In most developmental systems, gap junction mediated cell-cell communi
cation (GJC) can be detected from very early stages of embryogenesis.
This usually results in the entire embryo becoming linked as a syncyti
um. However, as development progresses, GJC becomes restricted at disc
rete boundaries, leading to the subdivision of the embryo into communi
cation compartment domains. Analysis of gap junction gene expression s
uggests that this functional subdivision of GJC may be mediated by the
differential expression of the connexin gene family. The temporal-spa
tial pattern of connexin gene expression during mouse embryogenesis is
highly suggestive of a role for gap junctions in inductive interactio
ns, being regionally restricted in distinct developmentally significan
t domains. Using reverse genetic approaches to manipulate connexin gen
e function, direct evidence has been obtained for the connexin 43 (Cx4
3) gap junction gene playing a role in mammalian development. The chal
lenges in the future are the identification of the target cell populat
ions and the cell signaling processes in which Cx43-mediated cell-cell
interactions are critically required in mammalian development. Our pr
eliminary observations suggest that neural crest cells may be one such
cell population.